# K260218: LacertaMatrix

- Pathway: 510(k) (Special)
- Applicant: Lacerta Life Sciences
- Decided: Feb 19, 2026 after 27 days
- Product code: KGN (Wound Dressing With Animal-Derived Material(S))
- Device class: U
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 10 generations back to K921895 (1992). 40 ancestors in all.
No later device cites it as a predicate yet.
0 of 41 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K252673: LacertaMatrix, Lacerta Life Science (2025) Summary page 5.

## Indications for use
LacertaMatrix is indicated for use in the management of the following wounds: • partial and full-thickness wounds • pressure ulcers • venous ulcers • diabetic ulcers • chronic vascular ulcers • tunneled / undermined wounds • surgical wounds (donor sites/grafts, post-Moh's surgery, post-laser surgery, podiatric, wound dehiscence) • trauma wounds (abrasions, lacerations, partial thickness burns, and skin tears) • draining wounds

Source page: https://510kreport.com/device/K260218
Methodology: https://510kreport.com/methodology